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Csv Engineer Jobs (NOW HIRING)

Eliquent Life Sciences, Inc

CSV Engineer

Mount Horeb, WI · On-site

$120K - $135K/yr

The CSV Engineer will author validation deliverables--including protocols, reports, and SOPs--ensuring compliance with FDA, EMA, and global regulatory expectations. Key Responsibilities: * Develop ...

Evotecgroup

IT CSV Engineer

Redmond, WA · On-site

$115K - $135K/yr

IT CSV Engineer Location: Seattle, WA OR Redmond, WA Reports to : Senior Manager/Group Leader, CSV About Us: At Just-Evotec, we believe that curiosity is the spark that drives innovation and success.

Evotec

IT CSV Engineer

Seattle, WA · On-site

$115K - $135K/yr

IT CSV Engineer Location: Seattle, WA OR Redmond, WA Reports to: Senior Manager/Group Leader, CSV About Us: At Just-Evotec, we believe that curiosity is the spark that drives innovation and success.

Nanda Technologies

CSV Engineer

Costa Mesa, CA · On-site

$55 - $60/hr

CSV Engineer Costa Mesa, CA or Seattle, WA(On-site) Visa: USC, GC & H4 EAD Key Responsibilities: * Develop and maintain Design Specifications (DS) for computerized and automated systems. * Author and ...

Evotec

IT CSV Engineer

Redmond, WA · On-site

$115K - $135K/yr

IT CSV Engineer Location: Seattle, WA OR Redmond, WA Reports to : Senior Manager/Group Leader, CSV About Us: At Just-Evotec, we believe that curiosity is the spark that drives innovation and success.

Evotec

IT CSV Engineer

Redmond, WA · On-site

$115K - $135K/yr

IT CSV Engineer Location: Seattle, WA OR Redmond, WA Reports to : Senior Manager/Group Leader, CSV About Us: At Just-Evotec, we believe that curiosity is the spark that drives innovation and success.

Forge USA

CSV Engineer I

Columbus, OH · On-site

CSV Engineer I At Forge Biologics, we believe in turning bold ideas into life-changing realities. Our mission is simple yet powerful: to enable access to life-changing gene therapies and help bring ...

Forge Biologics

CSV Engineer I

Columbus, OH · On-site

$67K - $86K/yr

The CSV Engineer I is responsible for ensuring that GxP computerized systems at Forge Biologics are validated in compliance with regulatory standards (21 CFR Part 11, EU Annex 11, GAMP 5). This role ...

Forge Biologics

CSV Engineer I

Columbus, OH · On-site

The CSV Engineer I is responsible for ensuring that GxP computerized systems at Forge Biologics are validated in compliance with regulatory standards (21 CFR Part 11, EU Annex 11, GAMP 5). This role ...

Noblesoft Technologies

CSV Engineer

Raritan, NJ · On-site

CSV Engineer Location: Raritan, NJ(Hybrid) Mandatory - Validation experience with ERP applications / SAP / MES • Experience in validating ERP/SAP/ MES Manufacturing applications • 3+ years ...

Forge Biologics

CSV Engineer I

Columbus, OH · On-site

The CSV Engineer I is responsible for ensuring that GxP computerized systems at Forge Biologics are validated in compliance with regulatory standards (21 CFR Part 11, EU Annex 11, GAMP 5). This role ...

Forge Biologics

CSV Engineer I

Columbus, OH · On-site

The CSV Engineer I is responsible for ensuring that GxP computerized systems at Forge Biologics are validated in compliance with regulatory standards (21 CFR Part 11, EU Annex 11, GAMP 5). This role ...

Forge Biologics

CSV Engineer I

Columbus, OH · On-site

$69K - $89K/yr

The CSV Engineer I is responsible for ensuring that GxP computerized systems at Forge Biologics are validated in compliance with regulatory standards (21 CFR Part 11, EU Annex 11, GAMP 5). This role ...

PCI Pharma Services

CSV Engineer III

Bedford, NH · On-site

$71K - $91K/yr

We're looking for a CSV Validation Engineer III to join our Quality and Compliance team. In this role, you'll take the lead in developing and executing validation strategies for GxP computer systems ...

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$36K

$99.4K

$137.5K

How much do csv engineer jobs pay per year?

As of Jun 5, 2026, the average yearly pay for csv engineer in the United States is $99,411.00, according to ZipRecruiter salary data. Most workers in this role earn between $77,000.00 and $116,500.00 per year, depending on experience, location, and employer.

What is a CSV Engineer job?

A CSV (Computer System Validation) Engineer is responsible for ensuring that computer systems used in regulated industries, such as pharmaceuticals and medical devices, comply with regulatory requirements. They develop validation protocols, perform testing, document results, and ensure adherence to industry standards like FDA 21 CFR Part 11 and GAMP 5. Their goal is to confirm that software and hardware systems function correctly, maintain data integrity, and meet compliance requirements.

What are the key skills and qualifications needed to thrive in the Csv Engineer position, and why are they important?

To thrive as a CSV Engineer (Computer System Validation Engineer), you need a solid understanding of validation principles, regulatory compliance (such as FDA 21 CFR Part 11), and a relevant degree in life sciences, engineering, or information technology. Familiarity with validation lifecycle documentation, risk assessment tools, and industry-standard systems like SAP, LIMS, and TrackWise is highly valued, as are certifications such as GAMP or Six Sigma. Strong attention to detail, analytical thinking, and excellent communication skills help CSV Engineers collaborate efficiently with cross-functional teams and ensure thorough documentation. These skills are crucial to guarantee that computerized systems in regulated industries meet compliance requirements, supporting product quality and patient safety.

What are the common challenges faced by a CSV Engineer in the pharmaceutical or medical device industry?

CSV Engineers in the pharmaceutical or medical device industry often face the challenge of keeping up with evolving regulatory requirements and ensuring all computerized systems remain compliant throughout their lifecycle. Managing comprehensive documentation, coordinating with multiple departments, and troubleshooting complex system changes can add to the workload. Successful CSV Engineers are proactive about staying informed of regulatory updates, are highly organized, and collaborate closely with Quality Assurance, IT, and operations teams. This dynamic environment offers the opportunity to learn continuously, develop expertise in validation best practices, and advance into leadership or specialized quality roles.
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Csv Engineer jobs near you
Infographic showing various Csv Engineer job openings in the United States as of May 2026, with employment types broken down into 4% Internship, 8% Full Time, 25% Part Time, 3% Temporary, 56% Contract, and 4% Nights. Highlights an 79% Physical, 4% Hybrid, and 17% Remote job distribution, with an average salary of $99,411 per year, or $47.8 per hour.

CSV Engineer

Katalyst Healthcares and Life Sciences

Pittsburgh, PA • On-site

Full-time

Posted yesterday

Job description

Job Summary:
  • CSV Engineer to support commissioning and validation activities for a newly built Cell & Gene Therapy R&D and manufacturing facility in Pittsburgh, PA.
  • The role focuses on reviewing validation deliverables, ensuring compliance with regulatory standards (21 CFR Part 11, GAMP 5), and coordinating with commissioning teams handling facilities, utilities, MES, EMS, CMMS, and related systems.
  • The consultant will work within environments using Kneat, Microsoft Office, and automation platforms such as MES and EMS/SMCS.
Roles & Responsibilities:
  • Review master validation plans and identify issues (CSV and CQV)
  • Verify scope, strategy, and acceptance criteri
  • Execute IQ/OQ/PQ protocols supporting commissioning of MES, Client, and associated equipment
  • Review commissioning and qualification protocols for CSV and CQV
  • Review functional and design specifications
  • Review SAT and FAT documentation
  • Review IQ/OQ/PQ protocols for URS alignment and accuracy
  • Ensure compliance with 21 CFR Part 11 and GAMP 5 (audit trails, access control, e-signatures)
  • Perform gap analysis of commissioning documentation to identify risks and deviations
  • ct as liaison between commissioning firm and internal Engineering, Quality, and IT teams
  • Review change control records and documentation
  • Manage validation data using Kneat
  • Support validation of MES, Client, EMS, or SMCS systems (e.g., SCADA, PLC, MES)
  • Create and execute CSV protocols
  • Manage traceability matrices
  • Create summary reports for approval
  • Manage deviations
  • Review FAT and SAT data for GMP compliance
  • Review automation system URS documentation
Experience:
  • Previous experience as a CSV Engineer supporting commissioning activities on life sciences construction projects (Greenfield or Brownfield)
  • Experience using Kneat for validation data management
  • Experience validating MES, Client, EMS, or SMCS systems
  • Experience creating/executing CSV IQ/OQ/PQ protocols
  • Experience managing traceability matrices
  • Experience preparing validation summary reports
  • Experience managing deviations
  • Experience reviewing FAT and SAT dat
  • Experience reviewing automation URS documents

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